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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Device

Roche Diagnostics Operations, Inc.: Due to low Quality Control recovery and invalid Calibration.

Agency Publication Date: October 16, 2019
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Affected Products

Product: Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 - Product Usage: In vitro test for the quantitative determination of the albumin in human serum and plasma on Roche/Hitachi cobas c systems.

Lot # 33962301. Expanded on 12/20/19 to include lot 37437301

Lot Numbers:
33962301
37437301
Product: Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Usage: In vitro test for the quantitative determination of the total bilirubin in serum and plasma of adults and neonates on Roche/Hitachi cobas c systems.

Lot # 36133801

Lot Numbers:
36133801

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 83806
Status: Resolved
Manufacturer: Roche Diagnostics Operations, Inc.
Manufactured In: United States
Units Affected: 2 products (7,032 units (Expanded on 12/20/19 to include 29,696 additional units); 2,304 units)
Agency Last Updated: December 31, 2019

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.